Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Kallanagouda R. Alagawadi"'
Publikováno v:
Medicinal Chemistry Research. 23:5160-5173
A series of 2-thioxothiazolidin-4-one derivatives were efficiently synthesized and evaluated for their cytotoxic activity against four tumor cell lines. The synthesized compounds were characterized by elemental analysis, IR, 1H NMR, 13C NMR, and mass
Publikováno v:
Journal of Heterocyclic Chemistry. 51:1705-1711
Condensation of coumarin-4-acetic acids (1) with ortho-phenylenediamine (2) in anhydrous phosphoric acid afforded 4-((1H-benzo[d]imidazol-2-yl)methyl)-2H-chromen-2-ones (3). Attempted Mannich reaction of 3 with formalin and primary amines resulted in
Publikováno v:
Medicinal Chemistry Research. 23:987-994
As a part of our continuation studies in developing new derivatives as dual antimicrobial/antitumor agents we describe the synthesis of new (Z)-2-(5-arylidene-2,4-dioxothiazolidin-3-yl) acetic acid derivatives (3a–m). The chemical structures of the
Publikováno v:
Letters in Drug Design & Discovery. 8:612-618
Publikováno v:
Medicinal Chemistry Research. 21:816-824
The present work describes the synthesis, antimicrobial and cytotoxic activity of 2,4-thiazolidinedione-5-acetic acid amides 3a–n. The structures of the compounds were confirmed by IR, 1H, 13C NMR and elemental analysis. All compounds were tested f
Autor:
Amol S. Shah, Pranali V. Sonkusare, Sagar M. Chaudhary, Dilip H. Dadwe, Kallanagouda R. Alagawadi, Shankar G. Alegaon
Publikováno v:
ChemInform. 43
A simple, highly efficient, cost effective, and environmentally benign synthesis of the title compounds (IX) (7 examples) and related analogues (XI), (XIII) is developed using microwave technique.
Autor:
Amol S. Shah, Shankar G. Alegaon, Pranali V. Sonkusare, Sagar M. Chaudhary, Kallanagouda R. Alagawadi, Dilip H. Dadwe
Publikováno v:
Bioorganicmedicinal chemistry letters. 22(5)
The increase in the prevalence of multi drug-resistant and extensively drug-resistant strains of Mycobacterium tuberculosis case demonstrates the urgent need of discovering new promising compounds with antimycobacterial activity. As part of our resea